HigherPurity™ Plant DNA Purification Kit

Référence AN0110-S

Conditionnement : 20rxn

Marque : Canvax Biotech

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Téléphone : +1 850 650 7790

HigherPurity™ Plant DNA Purification Kit

For a Highly Efficient, Convenient & Rapid Purification of Total DNA from a variety of Plant Tissues

HigherPurity™ Plant DNA Purification Kit offers a highly efficient, convenient and rapid method for purification of total DNA from a variety of plant tissues. The kit uses HigherPurity™ breakthrough technology based in DNA ability to bind silica in the presence of high concentrations of chaotropic salts.

SKU: AN0110 Categories: DNA & RNA Extraction, DNA Spin Column based Purification

Detailed information:

  • Highly efficient: yields up to 5˞-40 μg total DNA from young leaves.
  • Pure genomic DNA: ready-to-use in all Molecular Biology applications.
  • Really easy and fast procedure: it takes 56 minutes to get results with minimal handling steps.
  • Versatile: high quality DNA obtained from several types of plants.
  • Mini format.

Includes for 50 rxn:
– 50 DNAprep Spin Columns
– 50 Filter columns
– 100 Collection tubes (2 mL)
– 25 mL BL1 Buffer
– 7,5 mL BL2 Buffer
– 15 mL BL3 Buffer
– 13 mL Wash Buffer 1
– 15 mL Wash Buffer 2
– 10 mL Elution Buffer
– 480 uL RNase A Solution

Datasheet
MSDS

Purified DNA suitable for all common Molecular Biology applications, such as:

  • RT-PCR.
  • Southern blotting.
  • RFLP.

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  • Isolated from a 100 mg young leaf sample, quantified with a spectrophotometer and analysed by electrophoresis.
  • Recommendations: After addition of RNase A to Buffer S-I reagent can be stored at 4 ºC.
  • Shipped in: Ambient Temperature.
  • Storage: Room Temperature (15–25 °C). Store RNase A Solution at -20 °C
  • Christinaki, A. C., Myridakis, A. I., & Kouvelis, V. N. (2024). Genomic insights into the evolution and adaptation of secondary metabolite gene clusters in fungicolous species Cladobotryum mycophilum ATHUM6906G3: Genes, Genomes, Genetics14(4), jkae006.
  • Alexandra M Kortsinoglou, Martyn J Wood, Antonis I Myridakis, Marios Andrikopoulos, Andreas Roussis, Dan Eastwood, Tariq Butt, Vassili N Kouvelis, (2024) Comparative genomics of Metarhizium brunneum strains V275 and ARSEF 4556: unraveling intraspecies diversityG3 Genes|Genomes|Genetics,
  • García-Espinoza, F., García, M. J., Quesada-Moraga, E., & Yousef-Yousef, M. (2023). Entomopathogenic Fungus-Related Priming Defense Mechanisms in Cucurbits Impact Spodoptera littoralis (Boisduval) Fitness. Applied and Environmental Microbiology, e00940-23.
  • Fedoreyeva, L. I., Dilovarova, T. A., Vanyushin, B. F., Chaban, I. A., & Kononenko, N. V. (2022). Regulation of gene expression in Nicotiana tabacum seedlings by the MKASAA peptide through DNA methylation via the RdDM pathway. AIMS Biophysics9(2), 113-129.
  • Papaioannou, Charikleia, et al. “High Resolution Melting (HRM) Genotyping in the Genus Origanum: Molecular Identification and Discrimination for Authentication Purposes.”
  • Soffritti, G., Busconi, M., Sánchez, R. A., Thiercelin, J. M., Polissiou, M., Roldán, M., & Fernández, J. A. (2016). Genetic and Epigenetic Approaches for the Possible Detection of Adulteration and Auto-Adulteration in Saffron (Crocus sativus L.) SpiceMolecules21(3), 343.

This product is developed, designed and sold exclusively for Research purposes and in vitro use only (RUO). The product was not tested for use in diagnostics or for drug development, nor is it suitable for administration to humans or animals. For more info, please check its Material Safety Data Sheet available in this website.

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